Canonical Allele Identifier: CA2321045990

Gene: FCER2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7690506C= , CM000681.2:g.7690506C=	GRCh38
NC_000019.9:g.7755392C= , CM000681.1:g.7755392C=	GRCh37
NC_000019.8:g.7661392C=	NCBI36
NG_029554.1:g.16641G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597921.6:c.521G= MANE Select	ENSP00000471974.1:p.Cys174=
ENST00000346664.9:c.521G=	ENSP00000264072.6:p.Cys174=
ENST00000360067.8:c.518G=	ENSP00000353178.4:p.Cys173=
ENST00000593418.1:c.458G=	ENSP00000472067.1:p.Cys153=
ENST00000597312.5:n.1046G=
ENST00000597921.5:c.521G=	ENSP00000471974.1:p.Cys174=
ENST00000597934.1:n.883G=
ENST00000598803.5:n.1016G=
NM_001207019.2:c.518G=	NP_001193948.2:p.Cys173=
NM_001220500.1:c.521G=	NP_001207429.1:p.Cys174=
NM_002002.4:c.521G=	NP_001993.2:p.Cys174=
XM_005272462.3:c.521G=	XP_005272519.1:p.Cys174=
XM_005272462.4:c.521G=	XP_005272519.1:p.Cys174=
NM_001220500.2:c.521G= MANE Select	NP_001207429.1:p.Cys174=
NM_001207019.3:c.518G=	NP_001193948.2:p.Cys173=
NM_002002.5:c.521G=	NP_001993.2:p.Cys174=